Adhesive optical component comprising an adhesive composition

ABSTRACT

An adhesive optical component comprising an optical component and a layer which comprises an adhesive composition, the adhesive composition being disposed on at least one face of the optical component by coating a solution of the adhesive composition on the face of the optical component and drying the solution to form a laminate, the adhesive composition comprising (A) a copolymer of (meth)acrylic esters, (B) a crosslinking agent and (C) a phenol compound.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a Divisional application of application Ser. No.10/781,316 filed Feb. 17, 2004 (U.S. Pat. No. 7,179,528), which is aDivisional application of application Ser. No. 09/829,061 filed Apr. 9,2001 (U.S. Pat. No. 6,720,375).

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to an adhesive composition and an adhesiveoptical component using the adhesive composition. More particularly, thepresent invention relates to an adhesive composition which, byapplication to easily hydrolyzable materials such as substrates andadherends, suppresses degradation of the materials by hydrolysis andimproves durability of the materials; an adhesive composition whichprovides excellent stress relaxation without plasticizers, suppressesdegradation of easily hydrolyzable materials such as substrates andadherents by hydrolysis by application to the material, suppressesdegradation of the composition itself and gives adhesive opticalcomponents having excellent quality; and an adhesive optical componentcomprising the adhesive composition such as a polarizing plate and aplate for phase differentiation.

2. Description of Related Art

As the adhesive, acrylic adhesives, polyurethane adhesives, polyesteradhesives, rubber adhesives and silicone adhesives have heretofore beenused. Among these adhesives, acrylic adhesives are widely used. Anacrylic adhesive contains, in general, a copolymer of (meth)acrylicesters and a crosslinking agent. As the copolymer of (meth)acrylicesters, for example, a copolymer of a (meth)acrylic ester such asbutyl(meth)acrylate, 2-ethylhexyl(meth)acrylate, isooctyl(meth)acrylateand decyl(meth)acrylate with a functional monomer for formingcrosslinking points is used. The functional monomer is, specifically, afunctional monomer having hydroxyl group such ashydroxyethyl(meth)acrylate and hydroxypropyl(meth)acrylate or afunctional monomer having carboxyl group such as (meth)acrylic acid,maleic acid, crotonic and itaconic acid.

However, when the acrylic adhesive is applied to a material which iseasily hydrolyzed such as films of cellulose acetate, a problem arisesin that the material tends to be hydrolyzed due to the effect ofcarboxyl group in the copolymer of (meth)acrylic esters contained in theacrylic adhesive. The degradation of the material by hydrolysis takesplace markedly, in particular, under an environment of a hightemperature and high humidity.

Some optical components are used after a polarizing plate is attached tothe surface. Typical examples of such optical components include liquidcrystal cells in liquid crystal displays (LCD). In general, a liquidcrystal cell has a structure in which two transparent electrodesubstrates having an oriented layer are placed in a manner such that aspecific gap is formed between them with a spacer and the orientedlayers face to each other at the inside, peripheral portions of thetransparent electrode substrates are sealed, a liquid crystallinematerial is placed and held inside the gap between the transparentelectrode substrates and a polarizing plate is disposed on each outersurface of the two transparent electrode substrates via an adhesivelayer.

FIG. 1 shows a perspective view exhibiting the structure of an exampleof the polarizing plate described above. As shown in FIG. 1, thepolarizing plate 10 has a substrate having a three-layer structure inwhich triacetylcellulose (TAC) film I 2 and TAC film II 2′ are laminatedon the faces of a polarizing plate 1 made of polyvinyl alcohol. On oneface of the substrate, an adhesive layer 3 for sticking the substrate toan optical component such as a liquid crystal cell is formed. A releasesheet 4 is attached to the adhesive layer 3. In general, a film forprotecting the surface 5 is disposed on the face of the polarizing plateopposite to the face having the adhesive layer 3.

When the above polarizing plate is attached to the above liquid crystalcell, the release sheet 4 is removed first, then the polarizing plate isstuck to the liquid crystal cell via the exposed adhesive layer and thefilm for protecting the surface 5 is removed.

For the adhesive layer disposed on the polarizing plate, acrylicadhesives are widely used. However, as described above, the acrylicadhesive promotes hydrolysis of the TAC film of the polarizing plate dueto the effect of carboxyl group in the copolymer of (meth)acrylic estersand the polarizing plate is degraded. The degradation of the polarizingplate takes place markedly, in particular, under an environment of ahigh temperature and a high humidity.

In liquid crystal display apparatuses of the STN type, it is widelyconducted that a plate for phase differentiation is disposed between aliquid crystal cell and a polarizing plate. As the plate for phasedifferentiation, in general, a laminate having a TAC film on one or bothfaces of a stretched film of polyvinyl alcohol and a layer of an acrylicadhesive on the face of the TAC film, is used. An liquid crystal cell isformed by laminating one or a plurality of plates for phasedifferentiation to an STN cell via the above adhesive layer and thenlaminating a polarizing plate on the outermost layers. The thus preparedliquid crystal cell also has a problem in that degradation of the TACfilm by hydrolysis takes place in the plate for phase differentiationsimilarly to the degradation of the TAC film in the polarizing plate.

To overcome the above problems, for example, a method in which theamount of carboxyl group contained in the adhesive is decreased(Japanese Patent Application Laid-Open No. Showa 59(1984)-111114) and amethod in which a tertiary amine is added (Japanese Patent ApplicationLaid-Open No. Heisei 4(1992)-254803) have been proposed. However, themethod in which the amount of carboxyl group is decreased has a drawbackin that the excellent balance between the physical properties of theadhesive is inevitably lost and the method in which a tertiary amine isadded has a drawback in that the pot life of the adhesive decreasessince control of the reactions between a crosslinking agent and variousfunctional groups in the adhesive becomes difficult and workability invarious steps deteriorates.

The polarizing plate which is attached to the liquid crystal cell viathe adhesive layer has the three-layer structure described above. Due tothe properties of the materials, the polarizing plate has poordimensional stability and, in particular, change in the dimension bycontraction or expansion is great in the environment of a hightemperature or a high temperature and a high humidity.

However, since, in general, an adhesive having a great adhesive abilityis used in the above polarizing plate, stress caused by the change inthe dimension of the polarizing plate cannot be absorbed and relaxed bythe adhesive layer although lifting and peeling caused by the change inthe dimension of the polarizing plate can be suppressed. Morespecifically, in FIG. 1, TAC film II 2′ at the front face tends tocontract or expand due to change in the humidity and the temperature. Onthe other hand, TAC film I 2 cannot not contract or expand easily sinceTAC film I is firmly adhered to the liquid crystal cell via the adhesivelayer 3 and the adhesive layer cannot flexibly follow the change in thedimension. As the result, ray passing through TAC film I toward TAC filmII cannot proceed straight. This causes undesirable phenomena such asleak of light.

To overcome the above problems, heretofore, a plasticizer is added tothe adhesive so that the adhesive is flexible to a suitable degree andstress relaxation takes place. However, the adhesive containing aplasticizer has drawbacks in that the plasticizer bleeds out and thatthe adherend is stained with the plasticizer when the polarizing plateis peeled by the bleeding out. When a polyfunctional crosslinking agenthaving a functionality of three or greater is used in an adhesive, thenumber of crosslinks in the adhesive is decreased. However, the holdingability, i.e., the adhesion with the adherend, inevitably decreases inthis case and problems such as lifting and peeling of the polarizingplate tend to arise with passage of the time.

Intensive studies on adhesive compositions exhibiting excellent stressrelaxation without adding plasticizers have been made by the presentinventors to overcome the above problems and it was found that excellentstress relaxation can be exhibited by using a copolymer of (meth)acrylicesters having a great molecular weight and an oligomer of (meth)acrylicesters having a small molecular weight in combination. However, whenthis adhesive composition is applied to a polarizing plate and the like,it was found that an undesirable phenomenon occasionally took place inthat brightness was different at portions around the edges and at otherportions of the polarizing plate.

Moreover, a problem takes place in the acrylic adhesive in that themolecular weight of the copolymer of (meth)acrylic esters decrease sincedegradation takes place under a condition of a high temperature and ahigh humidity although the degradation proceeds slowly. As the result,cohesive force in the adhesive becomes insufficient and lifting andpeeling take place between a substrate such as a polarizing plate and aplate for phase differentiation and an adherend such as a plate of glassor polycarbonate.

SUMMARY OF THE INVENTION

Under the above circumstances, the present invention has a first objectof providing an adhesive composition which suppresses degradation ofeasily hydrolyzable materials by hydrolysis and improves durability ofthe materials when the adhesive composition is applied to the materials;a second object of providing an adhesive composition which providesexcellent stress relaxation without plasticizers, suppresses degradationof easily hydrolyzable materials by hydrolysis when the adhesivecomposition is applied to the materials, suppresses degradation of thecomposition itself and gives adhesive optical components havingexcellent quality; and a third object of providing an adhesive opticalcomponents such as a polarizing plate and a plate for phasedifferentiation which comprise a layer of the above adhesivecomposition.

As the result of intensive studies by the present inventors to achievethe above objects, it was found that the first object can be achievedwith an adhesive composition comprising a copolymer of (meth)acrylicesters, a crosslinking agents and a phenol derivative, that the secondobject can be achieved with an adhesive composition comprising acopolymer of (meth)acrylic esters or, preferably, a mixture of acopolymer of (meth)acrylic esters and an oligomer of (meth)acrylicesters, a crosslinking agent, a radical scavenger and, optionally, asecondary antioxidant and that the third object can be achieved bydisposing a layer comprising the adhesive composition obtained asdescribed above at least on one face of an optical component.

The present invention has been completed based on the above knowledge.

The present invention provides:

-   (1) An adhesive composition which comprises (A) a copolymer of    (meth)acrylic esters, (B) a crosslinking agent and (C) a phenol    derivative (referred to as adhesive composition I, hereinafter);-   (2) An adhesive optical component comprising an optical component    and a layer which comprises adhesive composition I and is disposed    at least on one face of the optical component (referred to as    Adhesive optical component I, hereinafter);-   (3) An adhesive composition which comprises (D) a copolymer of    (meth)acrylic esters having a weight-average molecular weight of    500,000 to 2,500,000, (E) a crosslinking agent and (F) a radical    scavenger (referred to as adhesive composition II, hereinafter);-   (4) An adhesive composition which comprises (D′) a mixture of a    copolymer of (meth)acrylic esters having a weight-average molecular    weight of 500,000 to 2,500,000 and an oligomer of (meth)acrylic    esters having a weight-average molecular weight of 1,000 to 10,000    in amounts such that a ratio of the amounts by weight of the    copolymer to the oligomer is in a range of 100:5 to 100:100, (E) a    crosslinking agent and (F) a radical scavenger (referred to as    adhesive composition II′, hereinafter); and-   (5) An adhesive optical component comprising an optical component    and a layer which comprises any of adhesive compositions II and    II′and is disposed at least on one face of the optical component    (referred to as Adhesive optical component II, hereinafter)

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a perspective view exhibiting the structure of an exampleof a polarizing plate.

In the figure, 1 means a polarizing plate made of polyvinyl alcohol, 2means TAC film I, 2′ means TAC film II, 3 means an adhesive layer, 4means a release sheet, 5 means a film for protecting the surface and 10means a polarizing plate.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

Adhesive composition I of the present invention will be described in thefollowing.

Adhesive composition I of the present invention comprises a copolymer of(meth)acrylic esters as component (A), a crosslinking agent as component(B) and a phenol derivative as component (C).

As the copolymer of (meth)acrylic esters of component (A), copolymershaving portions for crosslinking which can be crosslinked with thecrosslinking agent of component (B) are used. The copolymer of(meth)acrylic ester having such portions for crosslinking is notparticularly limited. A copolymer can be suitably selected fromcopolymers of (meth)acrylic esters which are conventionally used as theresin component of adhesives.

Preferable examples of the copolymer of (meth)acrylic ester having suchportions for crosslinking include copolymers of a (meth)acrylic ester inwhich the alkyl group in the ester portion has 1 to 20 carbon atoms, amonomer having a functional group having an active hydrogen and othermonomers which are used where desired.

Examples of the copolymer of a (meth)acrylic ester in which the alkylgroup in the ester portion has 1 to 20 carbon atoms includemethyl(meth)acrylate, ethyl(meth)acrylate, propyl(meth)acrylate,butyl(meth)acrylate, pentyl(meth)acrylate, hexyl(meth)acrylate,cyclohexyl(meth)acrylate, 2-ethylhexyl(meth)acrylate,isooctyl(meth)acrylate, decyl(meth)acrylate, dodecyl(meth)acrylate,myristyl(meth)acrylate, palmityl(meth)acrylate andstearyl(meth)acrylate. The copolymers of a (meth)acrylic ester may beused singly or in combination of two or more.

Examples of the monomer having a functional group having an activehydrogen include hydroxyalkyl esters of (meth)acrylic acid such as2-hydroxyethyl(meth)acrylate, 2-hydroxypropyl(meth)acrylate,3-hydroxypropyl(meth)acrylate, 2-hydroxybutyl(meth)acrylate,3-hydroxybutyl(meth)acrylate and 4-hydroxybutyl(meth)acrylate;acrylamides such as acrylamide, methacrylamide, N-methylacrylamide,N-methylmethacrylamide, N-methylolacrylamide andN-methylol-methacrylamide; monoalkylaminoalkyl(meth)acrylates such asmonomethylaminoethyl(meth)acrylate, monoethylaminoethyl(meth)acrylate,monomethylaminopropyl(meth)acrylate andmonoethyl-aminopropyl(meth)acrylate; and ethylenically unsaturatedcarboxylic acids such as acrylic acid, methacrylic acid, crotonic acid,maleic acid, itaconic acid and citraconic acid. The above monomers maybe used singly or in combination of two or more.

Examples of the other monomers which are used where desired includevinyl esters such as vinyl acetate and vinyl propionate; olefins such asethylene, propylene and isobutylene; halogenated olefins such as vinylchloride and vinylidene chloride; styrenic monomers such as styrene andα-methylstyrene; diene monomers such as butadiene, isoprene andchloroprene; nitrile monomers such as acrylonitrile andmethacrylonitrile; and N,N-dialkylsubstituted acrylamides such asN,N-dimethylacrylamide and N,N-dimethylmethacrylamide. The abovemonomers may be used singly or in combination of two or more.

In adhesive composition I of the present invention, the structure of thecopolymer of (meth)acrylic esters used as component (A) is notparticularly limited and any of random copolymers, block copolymers andgraft copolymers can be used. As for the molecular weight, it ispreferable that the weight-average molecular weight is in the range of500,000 to 2,500,000. When the weight-average molecular weight issmaller than 500,000, there is the possibility that adhesion anddurability of adhesion with the adherend are insufficient. When theweight-average molecular weight exceeds 2,500,000, the property offollowing change in the dimension of the substrate may deteriorate. Fromthe standpoint of adhesion, durability of adhesion and the property offollowing change in the dimension of the substrate, it is preferablethat the weight-average molecular weight is 800,000 to 1,800,000 andmore preferably 1,200,000 to 1,600,000.

The weight-average molecular weight described above is theweight-average molecular weight of the corresponding polystyreneobtained in accordance with the gel permeation chromatography (GPC).

In the present invention, the copolymer of (meth)acrylic esters ofcomponent (A) may be used singly or in combination of two or more. Wheredesired, homopolymers and copolymers of (meth)acrylic esters having asmall molecular weight such as a weight-average molecular weight of100,000 or smaller can be used in combination with the above copolymerof (meth)acrylic esters having a great molecular weight.

The crosslinking agent of component (B) in adhesive composition I of thepresent invention is not particularly limited. A compound can besuitably selected from crosslinking agents which are conventionally usedin acrylic adhesives. Examples of the crosslinking agent includepolyisocyanate compounds, epoxy resins, melamine resins, urea resins,dialdehydes and methylol polymers. In the present invention,polyisocyanate compounds are preferably used.

Examples of the polyisocyanate compound include aromatic polyisocyanatessuch as tolylene diisocyanate, diphenylmethane diisocyanate and xylylenediisocyanate; aliphatic polyisocyanates such as hexamethylenediisocyanate; alicyclic polyisocyanates such as isophorone diisocyanateand hydrogenated diphenylmethane diisocyanate; biuret compounds andisocyanurate compounds derived from the above polyisocyanates; andadduct compounds which are reaction products of the abovepolyisocyanates with low molecular weight compounds having an activehydrogen such as ethylene glycol, propylene glycol, neopentyl glycol,trimethylolpropane and castor oil.

In the present invention, the crosslinking agent of component (B) may beused singly or in combination of two or more. The amount is selected, ingeneral, in the range of 0.001 to 50 parts by weight and preferably inthe range of 0.01 to 10 parts by weight per 100 parts by weight of thecopolymer of acrylic esters of component (A) although the amount may bedifferent depending on the type of the crosslinking agent.

In adhesive composition I of the present invention, a phenol derivativeis used as component (C). The phenol derivative is used for suppressinghydrolysis of the easily hydrolyzable material such as a film ofacetylcellulose to which the adhesive composition of the presentinvention is applied.

As the phenol derivative, it is preferable that at least one compound issuitably selected, for example, from single ring phenol compounds,two-ring phenol compounds, three-ring phenol compounds and four-ringphenol compounds.

Examples of the phenol derivative include single ring phenol compoundssuch as 2,6-di-tert-butyl-p-cresol, butylhydroxyanisole and stearylβ-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate; two-ring phenolcompounds such as 4,4′-butylidenebis(3-methyl-6-tert-butylphenol) and3,6-dioxaoctamethylenebis[3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propionate];three-ring phenol compounds such as1,1,3-tris(2-methyl-4-hydroxy-5-tert-butylphenyl)butane; and four-ringphenol compounds such astetrakis[methylene-3-(3′,5′-di-tert-butyl-4′-hydroxyphenyl)propionate]-methane.

In the present invention, the amount of the phenol derivative ofcomponent (C) is selected, in general, in the range of 0.01 to 10 partsby weight per 100 parts by weight of the copolymer of (meth)acrylicesters of component (A). When the amount is less than 0.01 part byweight, there is the possibility that the effect of suppressinghydrolysis is not sufficiently exhibited and the object of the presentinvention is not achieved. When the amount exceeds 10 parts by weight,the effect of suppressing hydrolysis is not exhibited to the degreeexpected from the used amount. Moreover, economic disadvantage arisesand physical properties of adhesion may be adversely affected. From thestandpoint of the effect of suppressing hydrolysis, the physicalproperties of adhesion and the economy, it is preferable that the amountof the phenol derivative is in the range of 0.05 to 5 parts by weightand more preferably in the range of 0.1 to 2 parts by weight.

Adhesive composition I of the present invention may further comprisevarious additives conventionally used for adhesive compositions such asplasticizers, silane coupling agents and ultraviolet absorbents as longas the additives do not adversely affect the objects of the presentinvention, where desired.

When a silane coupling agent, among the above additives, is added to theadhesive composition, adhesion to a liquid crystal cell (glass) under ahot and humid condition is improved and lifting and peeling of thepolarizing plate and the plate for phase differentiation are suppressed.As the silane coupling agent, organic silicon compounds which have atleast one alkoxysilyl group in the molecule, are compatible with thecomponents of the adhesive composition and transmit light are preferablyused. For example, substantially transparent organic silicon compoundshaving these properties are used. Examples of the silane coupling agentinclude vinyltriethoxysilane, vinyltris(2-methoxyethoxy)silane,3-methacryloxypropyltrimethoxysilane, γ-glycidoxypropyltrimethoxysie,2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane,3-aminopropyltriethoxysilane and N-phenyl-3-aminopropyltrimethoxysilane.It is preferable that the amount of the silane coupling agent is in therange of 0.001 to 10 parts by weight and more preferably in the range of0.005 to 5 parts by weight per 100 parts by weight of the adhesivecomposition.

When adhesive composition I of the present invention having the abovecomposition is applied to easily hydrolyzable materials, degradation ofthe materials by hydrolysis is suppressed and, in particular, durabilityunder a high temperature and a high humidity can be improved. Therefore,adhesive composition I is advantageously applied to films ofacetylcellulose which are easily hydrolyzed.

Adhesive compositions II and II′ of the present invention will bedescribed in the following.

In adhesive composition II, a copolymer of (meth)acrylic esters alone isused as component (D) and, in adhesive composition II′, a mixture of acopolymer of (meth)acrylic esters and an oligomer of (meth)acrylicesters is used as component (D′).

As the copolymer of (meth)acrylic esters of component (D), a copolymerof (meth)acrylic esters having portions for crosslinking which can becrosslinked with the crosslinking agent of component (E) is used. Thecopolymer of (meth)acrylic esters having portions for crosslinking isnot particularly limited. A copolymer can be suitably selected fromcopolymers of (meth)acrylic esters which are conventionally used as theresin component of adhesive compositions.

Preferable examples of the copolymer of (meth)acrylic esters havingportions for crosslinking include copolymers of a (meth)acrylic ester inwhich the alkyl group in the ester portion has 1 to 20 carbon atoms, amonomer having a functional group having an active hydrogen and othermonomers which are used where desired.

Examples of the (meth)acrylic ester in which the alkyl group in theester portion has 1 to 20 carbon atoms, the monomer having a functionalgroup having an active hydrogen and the other monomers which are usedwhere desired include the (meth)acrylic ester in which the alkyl groupin the ester portion has 1 to 20 carbon atoms, the monomer having afunctional group having an active hydrogen and the other monomers whichare used where desired, respectively, which are described as theexamples of the components for the copolymer of (meth)acrylic esters ofcomponent (A) used in adhesive composition I.

In adhesive-composition II of the present invention, the structure ofthe copolymer of (meth)acrylic esters used as component (D) is notparticularly limited and any of random copolymers, block copolymers andgraft copolymers can be used. The weight-average molecular weight of thecopolymer is selected in the range of 500,000 to 2,500,000. When theweight-average molecular weight is smaller than 500,000, there is thepossibility that adhesion and durability of adhesion with the adherendare insufficient. When the weight-average molecular weight exceeds2,500,000, the property of following change in the dimension of thesubstrate may deteriorate. From the standpoint of adhesion, durabilityof adhesion and the property of following change in the dimension of thesubstrate, it is preferable that the weight-average molecular weight is800,000 to 1,800,000 and more preferably 1,200,000 to 1,600,000.

The weight-average molecular weight described above is theweight-average molecular weight of the corresponding polystyreneobtained in accordance with the gel permeation chromatography (GPC).

In the present invention, the copolymer of (meth)acrylic esters ofcomponent (D) may be used singly or in combination of two or more.

In adhesive composition II′ of the present invention, a mixture of thecopolymer of (meth)acrylic esters described above and an oligomer of(meth)acrylic esters can be used as component (D′) so that stressrelaxation is provided.

The oligomer of (meth)acrylic ester may be any oligomer selected fromoligomers obtained by homopolymerizing one compound selected from(meth)acrylic esters in which the alkyl group in the ester portion has 1to 20 carbon atoms, oligomers obtained by copolymerizing at least twocompounds selected from the above (meth)acrylic esters and oligomersobtained by copolymerizing at least one compound selected from the above(meth)acrylic esters with other monomers.

Examples of the (meth)acrylic ester in: which the alkyl group in theester portion has 1 to 20 carbon atoms and the other monomers includethe (meth)acrylic esters in which the alkyl group in the ester portionhas 1 to 20 carbon atoms and the other monomers, respectively, which aredescribed as the examples of the components for the copolymer of(meth)acrylic esters of component (A) used in adhesive composition I.

The weight-average molecular weight of the oligomer of (meth)acrylicesters is selected in the range of 1,000 to 10,000. When the molecularweight is smaller than 1,000, the oligomer bleeds out and there is thepossibility that an adherend is stained when a substrate adhered to theadherend via the adhesive composition is removed. When the molecularweight exceeds 10,000, there is the possibility that the property offollowing change in the dimension of the substrate (stress relaxation)of the adhesive composition deteriorates. From the standpoint ofpreventing staining of the adherend and the property of following changein the dimension of the substrate, it is preferable that theweight-average molecular weight of the oligomer of (meth)acrylic estersis in the range of 3,000 to 10,000.

It is preferable that the oligomer of (meth)acrylic esters has a ratioof the weight-average molecular weight (Mw) to the number-averagemolecular weight (Mn) representing the molecular weight distribution of2.0 or smaller. When the ratio Mw/Mn exceeds 2.0, there is thepossibility that the oligomer contains components having excessivelysmall molecular weights. Such components may cause bleeding out of theoligomer and staining of an adherend when a substrate adhered to theadherend via the adhesive composition is removed. It is more preferablethat the ratio Mw/Mn is 1.7 or smaller.

The weight-average molecular weight and the number-average molecularweight described above are the weight-average molecular weight and thenumber-average molecular weight, respectively, of the correspondingpolystyrene obtained in accordance with GPC.

In the present invention, the oligomer of (meth)acrylic esters may beused singly or in combination of two or more.

In adhesive composition II′ of the present invention, the oligomer of(meth)acrylic esters is used in an amount of 5 to 100 parts by weightper 100 parts by weight of the above copolymer of (meth)acrylic esters.When the amount of the oligomer is less than 5 parts by weight, theproperty of following change in the dimension of the substrate (stressrelaxation) becomes insufficient. When the amount of the oligomerexceeds 100 parts by weight, adhesion with the adherend becomes poor.From the standpoint of the property of following change in the dimensionof the substrate and adhesion with the adherend, it is preferable thatthe amount of the oligomer is in the range of 10 to 70 parts by weightand more preferably in the range of 15 to 50 parts by weight.

In adhesive compositions II and II′, the crosslinking agent of component(E) is not particularly limited. A crosslinking agent can be suitablyselected from conventional crosslinking agents used for acrylicadhesives. Examples of the crosslinking agent include the compoundsdescribed as the examples of the crosslinking agent of component (B) inadhesive composition I.

In the present invention, the crosslinking agent of component (E) may beused singly or in combination of two or more. The amount of thecrosslinking agent is selected, in general, in the range of 0.001 to 50parts by weight and preferably in the range of 0.01 to 10 parts byweight per 100 parts by weight of the copolymer of (meth)acrylic estersof component (D) or the copolymer of (meth)acrylic esters in component(D′) although the amount may be varied depending on the type of thecrosslinking agent.

Adhesive compositions II and II′ comprises a radical scavenger ascomponent (F).

The radical scavenger is a compound which scavenges radicals generatedby heat or light or with a heavy metal, suppresses initiation of chainreactions and inhibits chain reactions of the radicals. Since adhesivecompositions II and II′ of the present invention comprise the radicalscavenger, the following effects are exhibited:

-   (1) When adhesive compositions II and II′ are applied to an easily    hydrolyzable material such as a film of acetyl cellulose, hydrolysis    of the material is suppressed.-   (2) Degradation of the adhesive itself is suppressed and, even when    an optical component in which the adhesive composition of the    present invention is used is left standing under a condition of a    high temperature and a high humidity, lifting and peeling are not    easily formed.-   (3) When a copolymer of (meth)acrylic esters having a great    molecular weight and an oligomer of (meth)acrylic esters having a    small molecular weight are used in combination so that stress    relaxation is exhibited, formation of uneven brightness can be    suppressed in a polarizing plate to which the adhesive composition    of the present invention is applied.

In the present invention, antioxidants, amine photostabilizers andpolymerization inhibitors are preferably used as the radical scavenger.

As the antioxidant, phenolic antioxidants are preferable. Examples ofthe phenolic antioxidant include single ring phenol compounds such as2,6-di-t-butyl-p-cresol, 2,6-di-t-butyl-4-ethylphenol,2,6-dicyclohexyl-4-methylphenol, 2,6-diisopropyl-4-ethylphenol,2,6-di-t-amyl-4-methylphenol, 2,6-di-t-octyl-4-n-propylphenol, 2,6-dicyclohexyl-4-n-octylphenol, 2-isopropyl-4-methyl-6-t-butylphenol,2-t-butyl-4-ethyl-6-t-octylphenol, 2-isobutyl-4-ethyl-6-t-hexylphenol,2-cyclohexyl-4-n-butyl-6-isopropylphenol, mixed cresol modified withstyrene, DL-α-tocopherol and stearylβ-(3,5-di-t-butyl-4-hydroxyphenyl)propionate; two-ring phenol compoundssuch as 2,2′-methylenebis(4-methyl-6-t-butylphenol),4,4′-butylidenebis(3-methyl-6-t-butylphenol),4,4′-thiobis(3-methyl-6-t-butyl-phenol),2,2′-thiobis(4-methyl-6-t-butylphenol),4,4′-methylenebis(2,6-di-t-butylphenol),2,2′-methylenebis[6-(1-methylcyclohexyl)-p-cresol],2,2′-ethylidenebis(4,6-di-t-butylphenol),2,2′-butylidenebis(2-t-butyl-4-methylphenol),3,6-dioxaoctamethylenebis[3-(3-t-butyl-4-hydroxy-5-methylphenyl)propionate],triethyleneglycol bis[3-(3-t-butyl-5-methyl-4-hydroxyphenyl)propionate],1,6-hexanediol bis[3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate] and2,2′-thiodiethylenebis[3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate];three ring phenol compounds such as1,1,3-tris(2-methyl-4-hydroxy-5-t-butylphenyl)butane,1,3,5-tris(2,6-dimethyl-3-hydroxy-4-t-but1,3,5-tris[(3,5-di-t-butyl-4-hydroxy-phenyl)propionyloxyethyl]isocyanurate,tris(4-t-butyl-2,6-dimethyl-3-hydroxybenzyl)isocyanurate and1,3,5-trimethyl-2,4,6-tris(3,5-di-t-butyl-4-hydroxybenzyl)benzene;four-ring phenol compounds such astetrakis-[methylene-3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate]methane;and phenol compounds containing phosphorus such as bis(ethyl3,5-di-t-butyl-4-hydroxybenzylphosphonate)potassium and bis(ethyl3,5-di-t-butyl-4-hydroxybenzylphosphonate)nickel.

Examples of the amine photostabilizer includebis(2,2,6,6-tetramethyl-4-piperidyl) sebacate, polycondensates ofdimethyl succinate and 1- (2-hydroxyethyl)-4-hydroxy-2,2,6,6-tetramethylpiperidine, tetrakis (2,2,6,6-tetramethyl-4-piperidyl) -1,2,3,4-butanetetracarboxylate,2,2,6,6-tetramethyl-4-piperidyl benzoate,bis(1,2,6,6-pentamethyl-4-piperidyl) 2-(3,5-di-t-butyl-4-hydroxybenzyl)-2-n-butyl malonate, bis(N-methyl-2,2,6,6-tetramethyl-4-piperidyl)sebacate, 1,1′-(1,2-ethandiyl)-bis(3,3,5,5-tetramethylpiperadinone),(mixed 2,2, 6,6-tetramethyl-4-piperidyl/tridecyl)1,2,3,4-butanetetracarboxylate, (mixed1,2,2,6,6-pentamethyl-4-piperidyl/-tridecyl)1,2,3,4-butanetetracarboxylate, mixed[2,2,6,6-tetramethyl-4-piperidyl/β, β, β′,β′-tetramethyl-3,9-[2,4,8,10-tetraoxaspiro-(5,5)undecane]-diethyl]1,2,3,4-butanetetracarboxylate,mixed [1,2,2,6,6-pentamethy1-4-piperidyl/β, β, β′,β′-tetramethyl-3,9-[2,4,8,10-tetraoxaspiro-(5,5)undecane]-diethyl1,2,3,4-butanetetracarboxylate, condensates of N,N′-bis(3-aminopropyl)ethylenediamine and 2,4-bis[N-butyl-N-(1,2,2,6,6-penta-methyl-4-piperidyl)amino]-6-chloro-1,3,5-triazine,poly [6-N-morpholyl-1,3,5-triazin-2,4-yl][(2,2,6,6-tetramethyl-4-piperidyl) imino]hexa-methylene[(2,2,6,6-tetramethyl-4-piperidyl) imide], condensates of N,N′-bis(2,2,6,6-tetramethyl-4-piperidyl)hexamethylenediamine and1,2-dibromoethane and[N-(2,2,6,6-tetramethyl-4-piperidyl)-2-methyl-2-(2,2,6,6-tetramethyl-4-piperidyl)imino]propionamide.

The polymerization inhibitor is an agent conventionally used as thepolymerization inhibitor in radical polymerization. Examples of thepolymerization inhibitor include divalent phenolic polymerizationinhibitors such as hydroquinone, p-methoquinone, t-butylhydroquinone andt-butylcatechol; and phenothiazine.

In the present invention, the radical scavenger of component (F) may beused singly or in combination of two or more. The amount of the radicalscavenger is selected, in general, in the range of 0.01 to 10 parts byweight per 100 parts by weight of component (D) or component (D′). Whenthe amount is less than 0.01 part by weight, there is the possibilitythat the effect of the radical scavenger is not sufficiently exhibitedand the object of the present invention is not achieved. When the amountexceeds 10 parts by weight, the effect of the radical scavenger is notexhibited to the degree expected from the used amount. Moreover,economic disadvantage arises and physical properties of adhesion may beadversely affected. From the standpoint of the effect of the radicalscavenger, the physical properties of adhesion and the economy, it ispreferable that the amount of the radical scavenger is in the range of0.05 to 5 parts by weight and more preferably in the range of 0.1 to 2parts by weight.

When an antioxidant is used as the radical scavenger of component (F), apolymerizable antioxidant may be used in a manner such that thepolymerizable antioxidant is copolymerized in the preparation of thecopolymer of (meth)acrylic esters of component (D) or the copolymer of(meth)acrylic esters in component (D′) so that the unit of thepolymerizable antioxidant is incorporated into the prepared copolymer.In this case, the content of the unit of the polymerizable antioxidantis selected, in general, in the range of 0.01 to 10 parts by weight,preferably in the range of 0.05 to 5 parts by weight and most preferablyin the range of 0.1 to 2 parts by weight per 100 parts by weight of thetotal amount of component (D) or component (D′). By incorporating thepolymerizable antioxidant into the copolymer, the antioxidant does noteasily vaporize and an adhesive composition exhibiting excellentdurability can be obtained.

Examples of the polymerizable antioxidant include compounds (a), (b) and(c) having the following structures:

Compound (a) and compound (b) are commercially available as “SUMILIZERGM” [manufactured by SUMITOMO KAGAKU KOGYO Co., Ltd.] and “SUMILIZER GS”[manufactured by SUMITOMO KAGAKU KOGYO Co., Ltd.], respectively.

In adhesive compositions II and II′, a secondary antioxidant may be usedas component (G) in combination with the radical scavenger of component(F). When the radical scavenger is used alone, there is the possibilitythat the radical scavenger itself causes coloring. The secondaryantioxidant is used to suppress the coloring.

Examples of the secondary antioxidant include antioxidants containingphosphorus and antioxidants containing sulfur.

Examples of the antioxidant containing phosphorus include trioctylphosphite, trilauryl phosphite, tristridecyl phosphite, trisisodecylphosphite, phenyl diisooctyl phosphite, phenyl diisodecyl phosphite,phenyl di(tridecyl)phosphite, diphenyl isooctyl phosphite, diphenylisodecyl phosphite, diphenyl tridecyl phosphite, triphenyl phosphite,tris(nonylphenyl)phosphite, tris(2,4-di-t-butylphenyl)phosphite,tris(butoxyethyl)phosphite, tetratridecyl4,4′-butylidenebis(3-methyl-6-t-butylphenol)diphosphite,4,4′-isopropylidenediphenol alkyl phosphites (the alkyl group havingabout 12 to 15 carbon atoms),4,4′-isopropylidenebis(2-t-butylphenol)di(nonylphenyl)phosphite,tris(biphenyl)phosphite,tetra(tridecyl)1,1,3-tris(2-methyl-5-t-butyl-4-hydroxyphenyl)butanediphosphite, tris(3,5-di-t-butyl-4-hydroxyphenyl)phosphite, hydrogenated4,4′-isopropylidenediphenol polyphosphite, bis(octylphenyl)bis[4,4′-butylidenebis(3-methyl-6-t-butylphenol)]1,6-hexanedioldiphosphite, hexatridecyl1,1,3-tris(2-methyl-4-hydroxy-5-t-butylphenol)diphosphite,tris[4,4′-isopropylidenebis(2-t-butylphenol)]phosphite,tris(1,3-distearoyloxyisopropyl)phosphite,9,10-dihydro-9-phosphaphenanthrene-10-oxide,tetrakis(2,4-di-t-butylphenyl)-4,4′-biphenylene diphosphonite, distearylpentaerythritol diphosphite, di(nonylphenyl)pentraerythritoldiphosphite, phenyl 4,4,′-isopropylidenediphenol pentaerythritoldiphosphite, bis(2,4-di-t-butylphenyl)pentaerythritol diphosphite,bis(2,6-di-t-butyl-4-methylphenyl)pentaerythritol diphosphite andphenylbisphenol-A pentaerythritol diphosphite.

As the antioxidant containing sulfur, it is preferable that dialkylthiodipropionates and esters of alkylthiopropionic acids with polyhydricalcohols are used. As the dialkyl thiodipropionates, dialkylthiodipropionates having alkyl groups having 6 to 20 carbon atoms arepreferable. As the esters of alkylthiopropionic acids with polyhydricalcohols, esters of alkylthiopropionic having an alkyl group having 4 to20 carbon atoms with polyhydric alcohols are preferable. In this case,examples of the polyhydric alcohol for forming the ester of a polyhydricalcohol include glycerol, trimethylolethane, trimethylolpropane,pentaerythritol and trishydroxyethyl isocyanurate.

Examples of the dialkyl thiodipropionate include dilaurylthiodipropionate, dimyristyl thiodipropionate and distearylthiodipropionate. Examples of the ester of an alkylthiopropionic acidwith a polyhydric alcohol include glycerol tributylthiopropionate,glycerol trioctylthiopropionate, glycerol trilaurylthiopropionate,glycerol tristearylthiopropionate, trimethylolethanetributylthiopropionate, trimethylolethane trioctylthiopropionate,trimethylethane trilaurylthiopropionate, trimethylolethanetristearylthiopropionate, pentaerythritol tetrabutylthiopropionate,pentaerythritol tetraoctylthiopropionate, pentaerythritoltetralaurylthiopropionate and pentaerythritoltetrastearylthiopropionate.

In the present invention, the secondary antioxidant may be used singlyor in combination of two or more. The amount of the secondaryantioxidant is selected, in general, in the range of 0.1 to 10 parts byweight per 1 part by weight of the radical scavenger of component (F).When the amount is less than 0.1 part by weight, there is thepossibility that the effect of suppressing coloring is not sufficientlyexhibited. When the amount exceeds 10 parts by weight, the effect of thesecondary antioxidant is not exhibited to the degree expected from theused amount. Moreover, economic disadvantage arises and physicalproperties of adhesion may be adversely affected. From the standpoint ofthe effect of suppressing coloring, the physical properties of adhesionand the economy, it is preferable that the amount of the radicalscavenger is in the range of 0.5 to 5 parts by weight and morepreferably in the range of 1 to 2 parts by weight per 1 part by weightof the radical scavenger.

The adhesive compositions II and II′ of the present invention mayfurther comprise various additives conventionally used for adhesivecompositions such as plasticizers, silane coupling agents andultraviolet light absorbents as long as the objects of the presentinvention are not adversely affected, where desired,

When adhesive compositions II and II′ of the present invention havingthe above compositions are applied to easily hydrolyzable materials,degradation of the materials by hydrolysis is suppressed and, inparticular, durability under the environment of a high temperature and ahigh humidity can be improved. Therefore, it is advantageous that theadhesive compositions of the present invention are applied to films ofacetyl cellulose which are easily hydrolyzed.

When adhesive compositions I, II and II′ are used for opticalcomponents, it is advantageous that the compositions transmit light.

In the present invention, a layer comprising any of adhesivecompositions I, II and II′ (referred occasionally to as an adhesivelayer, hereinafter) can be disposed at least on one face of a substrateand the obtained laminate can be used as an adhesive sheet. Examples ofthe substrate include paper substrates such as glassine paper, coatedpaper and cast paper; laminate papers obtained by laminatingthermoplastic resins such as polyethylene on the paper substrates;polyester films such as films of polyethylene terephthalate,polybutylene phthalate and polyethylene naphthalate; polyolefin filmssuch as films of polypropylene and polymethylpentene; plastic films suchas films of polycarbonate and cellulose acetate; and laminate sheetscontaining these films. The substrate is suitably selected in accordancewith the application of the adhesive sheet.

The above adhesive sheet can be used for transferring the adhesive layerto an adherend or as a component stuck to a desired adherend. When theadhesive sheet is used in the former application, in general, asubstrate sheet is coated with a release agent such as a silicone resin.In this case, the thickness of the substrate sheet is not particularlylimited. In general, the thickness is 20 to 150 μm.

When the adhesive sheet is used in the latter application, the type andthe thickness of the substrate are suitably selected in accordance withthe application. A conventional release sheet may be disposed on theadhesive layer, where desired.

In the above adhesive sheets, the thickness of the adhesive layer is, ingeneral, about 5 to 150 μm and preferably about 10 to 90 μm.

The adhesive optical components I and II of the present inventioncomprises an optical component and a layer which comprises any ofadhesive compositions I, II and II′ and is disposed at least on one faceof the optical component.

Preferable examples of the above optical component include polarizingplates and plates for phase differentiation each having a TAC film.Examples of the above polarizing plates include polarizing plates usedfor liquid crystal display apparatuses, for adjustment of quantity oflight, for apparatuses using interference of polarized light and foroptical detectors of defects.

As the application of adhesive optical components I and II of thepresent invention, in particular, it is preferable that the layerscomprising adhesive compositions I, II and II′ are disposed onpolarizing plates and plates for phase differentiation for liquidcrystal cells in liquid crystal display apparatuses.

When the adhesive composition I of the present invention is applied toeasily hydrolyzable materials, degradation of the materials byhydrolysis can be suppressed and durability can be improved. Therefore,when the adhesive composition is applied to polarizing plates and platesfor phase differentiation for liquid crystal cells, hydrolysis of theTAC film disposed in the plates is suppressed and, in particular,durability under the environment of a high temperature and a highhumidity can be improved.

Adhesive compositions II and II′ provide excellent stress relaxationwithout plasticizers. Moreover, when the compositions are applied toeasily hydrolyzable materials, adhesive optical components havingexcellent qualities can be provided since degradation of the materialsby hydrolysis can be suppressed and degradation of the adhesivecompositions themselves can also be suppressed.

EXAMPLES

The present invention will be described more specifically with referenceto examples in the following. However, the present invention is notlimited to the examples.

Example 1

Into 200 parts by weight of toluene, 100 parts by weight of a copolymerof acrylic esters having a weight-average molecular weight of 1,200,000(the unit of butyl acrylate: 97% by weight and the unit of acrylic acid:3% by weight), 0.05 parts by weight of an adduct of trimethylolpropaneand tolylene diisocyanate as the crosslinking agent and 0.5 parts byweight of 2,6-di-tert-butyl-p-cresol as the phenol derivative were addedand a solution of an adhesive was prepared.

A substrate of a polyethylene terephthalate film having a thickness of38 μm which was coated with a silicone resin on one face [manufacturedby LINTEC Corporation; the trade name: SP PET38] was coated with thesolution of an adhesive prepared above on the face coated with asilicone resin. The substrate coated with the solution of an adhesivewas dried at 100° C. for 1 minute and an adhesive sheet having anadhesive layer having a thickness of 30 μm was prepared.

The prepared adhesive sheet was laminated to one face of a TAC filmhaving a thickness of 80 μm in a manner such that the adhesive layer wasattached to the TAC film. The obtained laminate was aged at the ordinarytemperature for one week and an adhesive optical component having alength of 80 mm and a width of 150 mm was prepared.

The substrate on the adhesive optical component prepared above wasremoved and the remaining adhesive optical component was stuck to aglass substrate via the exposed adhesive layer.

The obtained product was subjected to the durability tests under thecondition of a high temperature and under the condition of a hightemperature and a high humidity shown below and the properties wereevaluated. No degradation of the TAC film was confirmed. No lifting orpeeling from the glass substrate was found.

<Evaluation of the Properties of the Optical Component>

The durability tests were conducted under a condition of a hightemperature of 100° C. and dry and under a condition of a hightemperature of 80° C. and a high humidity of 90% RH. The degradation ofthe TAC film (turbidity and coloring) and lifting and peeling from theglass substrate were visually observed and the properties of the opticalcomponent were evaluated.

Examples 2 to 7

Optical components were prepared and the properties were evaluated inaccordance with the same procedures as those conducted in Example 1except that compounds shown in Table 1 were used in amounts shown inTable 1 as the phenol derivative in place of 2,6-di-tert-butyl-p-cresol.The results are shown in Table 1.

In Table 1, the phenol derivatives are abbreviated as shown in thefollowing:

C-1: butylhydroxyanisole

C-2: stearyl β-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate

C-3: 4,4′-butylidenebis(3-methyl-6-tert-butylphenol)

C-4: 3,6-dioxaoctamethylenebis[3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propionate]

C-5: 1,1,3-tris(2-methyl-4-hydroxy-5-tert-butylphenyl)butane

C-6: tetrakis [methylene-3-(3′,5′-di-tert-butyl-4′-hydroxyphenyl)propionate]methane

TABLE 1 Evaluation of properties high Phenol derivative temperatureamount high and type (part by wt.) temperature high humidity Example 2C-1 1.5 good good Example 3 C-2 2.0 good good Example 4 C-3 0.5 goodgood Example 5 C-4 0.5 good good Example 6 C-5 0.5 good good Example 7C-6 0.5 good good Note: good means that no degradation of a TAC film wasconfirmed and no lifting or peeling from a glass substrate was formed.

Example 8

Into 300 parts by weight of toluene, 100 parts by weight of thecopolymer of acrylic esters which was used in Example 1, 50 parts byweight of a homopolymer of butyl acrylate having a weight-averagemolecular weight of 50,000, 0.05 parts by weight of an adduct oftrimethylolpropane and tolylene diisocyanate as the crosslinking agentand 0.5 parts by weight of 2,6-di-tert-butyl-p-cresol as the phenolderivative were added and a solution of an adhesive was prepared.

Subsequently, the same procedures as those conducted in Example 1 wereconducted. Under the condition of a high temperature and a highhumidity, no degradation of the TAC film was confirmed and no lifting orpeeling from the glass substrate was found.

Example 9

A solution of an adhesive was prepared in accordance with the sameprocedures as those conducted in Example 1 except that 0.05 parts byweight of γ-glycidoxypropyltrimethoxysilane, which is a silane couplingagent, was further added.

Subsequently, the same procedures as those conducted in Example 1 wereconducted. Under the condition of a high temperature and a highhumidity, no degradation of the TAC film was confirmed and no lifting orpeeling from the glass substrate was found.

Comparative Example 1

The same procedures as those conducted in Example 1 were conductedexcept that 2,6-di-tert-butyl-p-cresol was not added. In the durabilitytests under the condition of a high temperature and under the conditionof a high temperature and a high humidity, the TAC film became turbidunder the condition of a high temperature and a high humidity andpeeling from the glass substrate took place under the condition of ahigh humidity.

Example 10

Into 200 parts by weight of toluene, 100 parts by weight of a copolymerof acrylic esters having a weight-average molecular weight of 1,200,000(the unit of butyl acrylate: 97% by weight and the unit of acrylic acid:3% by weight), 0.05 parts by weight of an adduct of trimethylolpropaneand modified tolylene diisocyanate as the crosslinking agent and 0.1part by weight of 2,6-di-tert-butyl-p-cresol as the radical scavenger ofa phenolic antioxidant were added and a solution of an adhesive wasprepared.

A release sheet of a polyethylene terephthalate film having a thicknessof 38 μm which was coated with a silicone resin on one face[manufactured by LINTEC Corporation; the trade name: SP PET38] wascoated with the solution of an adhesive prepared above on the facecoated with a silicone resin. The release sheet coated with the solutionof an adhesive prepared above was dried at 100° C. for 1 minute and anadhesive sheet having an adhesive layer having a thickness of 30 μm wasprepared.

The prepared adhesive sheet was laminated to one face of a polarizingplate having a three-layer laminate structure composed of a film oftriacetylcellulose, a film of polyvinyl alcohol and a film oftriacetylcellulose laminated in this order in a manner such that thelayer of the adhesive was attached to the polarizing plate. The obtainedlaminate was aged at the ordinary temperature for one week and anadhesive optical component having a length of 80 mm and a width of 150mm was prepared.

The release sheet on the adhesive optical component prepared above wasremoved and the remaining adhesive optical component was stuck to bothfaces of a glass plate for a liquid crystal cell via the exposedadhesive layer so that an orthogonal Nicol was formed.

The properties of the obtained optical component was evaluated inaccordance with the methods described in the following. The results ofthe evaluation are shown in Table 2.

<Evaluation of the Properties of the Optical Component>

The durability tests were conducted under the condition of a hightemperature of 100° C. and dry for 1,000 hours and under the conditionof a high temperature of 80° C. and a high humidity of 90% RH for 1,000hours. The results were evaluated as follows:

(1) Resistance of a TAC Film to Hydrolysis

The condition of degradation (turbidity and coloring) of a TAC film wasevaluated by visual observation. When no lifting or peeling was found,the resistance to hydrolysis was evaluated as good. When lifting andpeeling were found, the resistance to hydrolysis was evaluated as poor.

(2) Durability (Resistance of an Adhesive to Degradation)

The presence or the absence of lifting and peeling of an opticalcomponent from a glass plate was visually observed. When no lifting orpeeling was found, the durability was evaluated as good. When liftingand peeling were found, the durability was evaluated as poor.

(3) Effect of Suppressing Difference in Brightness

Difference in brightness at peripheral portions and at inner portions(the picture frame phenomenon) of a polarizing plate was visuallyobserved. When no picture frame phenomenon, i.e., no difference inbrightness, was found, the effect of suppressing difference inbrightness was evaluated as good. When the picture frame phenomenon,i.e., the difference in brightness, was found, the effect of suppressingdifference in brightness was evaluated as poor.

(4) Resistance to Coloring of an Adhesive

An adhesive layer was formed on a polarizing plate and the resultantlaminate was stuck to a glass plate. The obtained optical component wasplaced under the condition of a high temperature of 100° C. and dry for1,000 hours or under the condition of a high temperature of 80° C. and ahigh humidity of 90% RH for 1,000 hours. The change in color of theoptical component was obtained by the measurement of the degree ofyellowing (b*) and the degree of redding (c*) in accordance with themethod of Japanese Industrial Standard K 7103 using a. color differencemeter [manufactured by NIPPON DENSHOKU Co., Ltd.; SQ-2000]. Theresistance to coloring was evaluated in accordance with the followingcriteria:

-   -   good: a change smaller than 0.5    -   fair: a change of 0.5 or greater and smaller than 1.0    -   poor: a change of 1.0 or greater

Example 11

An optical component was prepared and evaluated in accordance with thesame procedures as those conducted in Example 10 except that 0.1 part byweight of an antioxidant containing phosphorus which was a4,4′-isopropylidenediphenol alkyl phosphite [manufactured by ASAHI DENKAKOGYO Co., Ltd.; the trade name: ADEKASTAB 1500] was further added asthe secondary antioxidant. The results are shown in Table 2.

Example 12

An optical component was prepared and evaluated in accordance with thesame procedures as those conducted in Example 10 except that 25 parts byweight of a homooligomer of -butyl acrylate having a weight-averagemolecular weight of 4,000 (Mw/Mn=1.5) and 0.05 parts by weight of theantioxidant containing phosphorus used in Example 11 [ADEKASTAB 1500]were further added. The results are shown in Table 2.

Example 13

An optical component was prepared and evaluated in accordance with thesame procedures as those conducted in Example 12 except that 0.05 partsby weight of an antioxidant containing sulfur which was dimyristylthiodipropionate [manufactured by ASAHI DENKA KOGYO Co., Ltd.; the tradename: ADEKASTAB AO-503A] was used in place of the antioxidant containingphosphorus “ADEKASTAB 1500”. The results are shown in Table 2.

Example 14

An optical component was prepared and evaluated in accordance with thesame procedures as those conducted in Example 10 except that 25 parts byweight of a homooligomer of butyl acrylate having a weight-averagemolecular weight of 10,000 (Mw/Mn=1.6) was further added and 0.1 part byweight of a phenolic antioxidant [manufactured by SUMITOMO KAGAKU KOGYOCo., Ltd.; the trade name: SUMILIZER GS] was used in place of 0.1 partby weight of 2,6-di-t-butyl-p-cresol. The results are shown in Table 2.

Example 15

An optical component was prepared and evaluated in accordance with thesame procedures as those conducted in Example 14 except that 0.05 partsby weight of an amine photostabilizer which wastetrakis(2,2,6,6-tetramethyl-4-piperidyl)-1,2,3,4-butanetetracarboxylate[manufactured by ASAHI DENKA KOGYO Co., Ltd.; the trade name: ADEKASTABLA-57]was used in place of 0.1 part by weight of the phenolicantioxidant “SUMILIZER GS”. The results are shown in Table 2.

Example 16

An optical component was prepared and evaluated in accordance with thesame procedures as those conducted in Example 15 except that 0.05 partsby weight of an antioxidant containing phosphorus which wasbis(2,6-di-t-butyl-4-methylphenyl)pentaerythritol diphosphite[manufactured by ASAHI DENKA KOGYO Co., Ltd.; the trade name: ADEKASTABPEP-36] was further added. The results are shown in Table 2.

Example 17

An optical component was prepared and evaluated in accordance with thesame procedures as those conducted in Example 10 using 100 parts byweight of a copolymer of acrylic esters having a weight-averagemolecular weight of 1,200,000 (the unit of butyl acrylate: 96.9% byweight, the unit of acrylic acid: 3% by weight and the unit of apolymerizable phenolic antioxidant [manufactured by SUMITOMO KAGAKUKOGYO Co., Ltd.; the trade name: SUMILIZER GM]: 0.1% by weight), 25parts by weight of a homooligomer of butyl acrylate having aweight-average molecular weight of 10,000, 0.05 parts by weight of anadduct of trimethylolpropane and modified tolylene diisocyanate and 0.05parts by weight of the antioxidant containing phosphorus “ADEKASTAB1500” which was used above. The results are shown in Table 2.

Example 18

An optical component was prepared and evaluated in accordance with thesame procedures as those conducted in Example 10 except that 0.5 partsby weight of hydroquinone which was a polymerization inhibitor was usedin place of 0.1 part by weight of 2,6-di-t-butyl-p-cresol. The resultsare shown in Table 2.

Comparative Example 2

An optical component was prepared and evaluated in accordance with thesame procedures as those conducted in Example 10 except that2,6-di-t-butyl-p-cresol was not used. The results are shown in Table 2.

Comparative Example 3

An optical component was prepared and evaluated in accordance with thesame procedures as those conducted in Example 12 except that either2,6-di-t-butyl-p-cresol or the antioxidant containing phosphorus“ADEKASTAB 1500” was not used. The results are shown in Table 2.

TABLE 2 Evaluation of properties of optical component effect ofresistance to suppressing resistance to hydrolysis of difference incoloring of TAC film durability brightness adhesive Example 10 good goodgood fair Example 11 good good good good Example 12 good good good goodExample 13 good good good good Example 14 good good good good Example 15good good good fair Example 16 good good good good Example 17 good goodgood good Example 18 good good good fair Comparative poor poor good goodExample 2 Comparative poor poor poor good Example 3

In Examples 10 to 18, the resistance to hydrolysis of a TAC film, thedurability and the effect of suppressing difference in brightness weregood. In Examples 11 to 14, 16 and 17, the resistance to coloring of anadhesive was good. In Example 14, although the phenolic antioxidant wasused alone without secondary antioxidants, the resistance to coloring ofan adhesive was good since the specific antioxidant causing littlecoloring was used. In Example 17, the polymerizable antioxidant was usedas the phenolic antioxidant and introduced into the copolymer of acrylicesters by copolymerization. The optical component exhibiting excellentproperties could be obtained.

In contrast, in Comparative Examples 2 and 3, hydrolysis of the TAC filmtook place and coloring of the film was observed since no antioxidantswere added. Portions of the adhesive optical component were peeled fromthe glass plate. In Comparative Example 3, the difference in brightnesswas found in the polarizing plate.

1. An adhesive optical component comprising an optical component and alayer which comprises an adhesive composition, said adhesive compositionbeing disposed on at least one face of the optical component by coatinga solution of the adhesive composition on said face of the opticalcomponent and drying the solution to form a laminate, said adhesivecomposition comprising (A) a copolytner of (meth)acrylic esters, (B) acrosslinking agent and (C) at least one phenol compound which isselected from the group consisting of 2,6-di-tert-butyl-p-cresol,butylhydroxyanisole, stearylβ-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate,4,4′-butylidenebis(3-methyl-6-tert-butylphenol),3,6-dioxaoctamethylenebis-[3-(3-tert-butyl-4-hydroxy-5-methyl-phenyl)propionate]and 1,1,3-tris(2-methyl-4-hydroxy-5-tert-butylphenyl)butane, wherein thecrosslinking agent (B) is in an amount of 0.001 to 50 parts by weightper 100 parts by weight of component (A).
 2. An adhesive opticalcomponent comprising an optical component and a layer which comprises anadhesive composition, a solution of said adhesive composition beingdisposed on one face of a substrate, said face of said substrate beingcoated with a releasing agent, drying the solution to form a laminateand transferring the adhesive composition to said face of the opticalcomponent, said adhesive composition comprising (A) a copolymer of(meth)acrylic esters, (B) a crosslinking agent and (C) a phenol compoundwhich comprises at least one compound selected from the group consistingof 2,6-di-tert-butyl-p-cresol, butylhydroxyanisole, stearylβ-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate,4,4′-butylidenebis(3-methyl-6-tert-butylphenyl),3,6-dioxaoctamethylenebis-[3-(3-tert-butyl-4-hydroxy-5-methylphenyl)-propionate]and1,1,3-tris (2-methyl-4-hydroxy-5-tert-butylphenyl)butane, wherein thecrosslinking agent (B) is in an amount of 0.001 to 50 parts by weightper 100 parts by weight of component (A).
 3. The adhesive opticalcomponent according to claim 2, wherein the adhesive compositioncomprises 0.01 to 10 parts by weight of the phenol compound (C) per 100parts by weight of component (A).
 4. The adhesive optical componentaccording to claim 2, wherein the optical component is a polarizingplate.
 5. The adhesive optical component according to claim 2, whereinthe optical component is a plate for phase differentiation.
 6. Theadhesive optical component according to claim 2, wherein after drying,the laminate is aged at ordinary temperature for at least a week.
 7. Theadhesive optical component according to claim 2, wherein the copolymerof (meth)acrylic esters (A) is a copolymer of (a) at least one monomerselected from the group consisting of methyl (meth) acrylate, ethyl(meth) acrylate, propyl (meth) acrylate, butyl (meth)acrylate, pentyl(meth)acrylate, hexyl(meth)acrylate and cyclohexyl (meth)acrylate, and(b) at least one monomer selected from the group consisting of2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate,3-hydroxypropyl (meth)acrylate, 2-hydroxybutyl (meth) acrylate,3-hydroxybutyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate,acrylamide, methacrylamide, N-methylacrylamide, N-met hylmethacrylamide,N-methylolacrylamide, N-methylolmethacrylamide, monomethylaminoethyl(meth) acrylate, monoethylaminoethyl (meth) acrylate,monomethylaminopropyl (meth) acrylate, monoethylaminopropyl (meth)acrylate, acrylic acid, methacrylic acid; crotonic acid, maleic acid,itaconic acid and citraconic acid.
 8. The adhesive optical componentaccording to claim 7, wherein the crosslinking agent (B) is apolyisocyanate compound.
 9. The adhesive optical component according toclaim 8, wherein the phenol compound (C) is selected from the groupconsisting of 2,6-di-tert-butyl-p-cresol and 4,4′-butylidenebis(3-methyl-6-tert-butylphenol).
 10. The adhesive optical componentaccording to claim 2, wherein the copolymer of (meth)acrylic ester (A)is a copolymer of butyl acrylate and acrylic acid.